Position Summary:
The Associate Director Clinical Operations will provide strategic and operational leadership for early-phase clinical trials with a primary focus on Phase 1 and Phase 2 studies within Immunology and Autoimmune therapeutic areas. This role is responsible for overseeing clinical trial execution from study start-up through close-out ensuring timelines quality compliance and budget objectives are met. The Associate Director will collaborate cross-functionally with internal teams CROs and external partners to drive successful clinical outcomes.
This position is mostly remote with infrequent travel to Germantown MD.
Responsibilities:
- Lead and oversee Phase 1 and Phase 2 clinical trials in Immunology and Autoimmune indications.
- Provide operational leadership for study planning start-up execution and close-out activities.
- Develop and manage clinical timelines budgets and resource plans.
- Serve as the primary operational point of contact for CROs vendors and clinical sites.
- Ensure clinical trials are conducted in compliance with ICH-GCP FDA regulations and applicable global regulatory requirements.
- Collaborate closely with Clinical Development Regulatory Affairs Data Management Biostatistics Pharmacovigilance and Medical Affairs teams.
- Review and contribute to clinical protocols informed consent forms (ICFs) clinical study reports (CSRs) and regulatory submissions.
- Oversee site selection site initiation monitoring strategy and issue escalation and resolution.
- Identify operational risks and implement mitigation strategies to ensure trial success.
- Mentor and provide guidance to Clinical Operations staff and cross-functional team members.
- Support inspection readiness activities and participate in audits and regulatory inspections as needed.
Required Experience:
Director
Position Summary:The Associate Director Clinical Operations will provide strategic and operational leadership for early-phase clinical trials with a primary focus on Phase 1 and Phase 2 studies within Immunology and Autoimmune therapeutic areas. This role is responsible for overseeing clinical trial...
Position Summary:
The Associate Director Clinical Operations will provide strategic and operational leadership for early-phase clinical trials with a primary focus on Phase 1 and Phase 2 studies within Immunology and Autoimmune therapeutic areas. This role is responsible for overseeing clinical trial execution from study start-up through close-out ensuring timelines quality compliance and budget objectives are met. The Associate Director will collaborate cross-functionally with internal teams CROs and external partners to drive successful clinical outcomes.
This position is mostly remote with infrequent travel to Germantown MD.
Responsibilities:
- Lead and oversee Phase 1 and Phase 2 clinical trials in Immunology and Autoimmune indications.
- Provide operational leadership for study planning start-up execution and close-out activities.
- Develop and manage clinical timelines budgets and resource plans.
- Serve as the primary operational point of contact for CROs vendors and clinical sites.
- Ensure clinical trials are conducted in compliance with ICH-GCP FDA regulations and applicable global regulatory requirements.
- Collaborate closely with Clinical Development Regulatory Affairs Data Management Biostatistics Pharmacovigilance and Medical Affairs teams.
- Review and contribute to clinical protocols informed consent forms (ICFs) clinical study reports (CSRs) and regulatory submissions.
- Oversee site selection site initiation monitoring strategy and issue escalation and resolution.
- Identify operational risks and implement mitigation strategies to ensure trial success.
- Mentor and provide guidance to Clinical Operations staff and cross-functional team members.
- Support inspection readiness activities and participate in audits and regulatory inspections as needed.
Required Experience:
Director
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